Počet záznamov: 1
von Hippelova-Lindauova choroba
SYS d006623 LBL 00000cx--j2200000---45-- 005 20240119195717.5 100 $a 19990101asloy0103----ba0 152 $b mesh 250 $a von Hippelova-Lindauova choroba $x BL $x CF $x CI $x CL $x CO $x DG $x DH $x DI $x DT $x EC $x EH $x EM $x EN $x EP $x ET $x GE $x HI $x IM $x ME $x MI $x MO $x NU $x PA $x PC $x PP $x PS $x PX $x RH $x RT $x SU $x TH $x UR $x VE $x VI $8 slo 300 1-
$a 2008 (1975) $8 eng 330 1-
$a An autosomal dominant disorder caused by mutations in a tumor suppressor gene. This syndrome is characterized by abnormal growth of small blood vessels leading to a host of neoplasms. They include HEMANGIOBLASTOMA in the RETINA; CEREBELLUM; and SPINAL CORD; PHEOCHROMOCYTOMA; pancreatic tumors; and renal cell carcinoma (see CARCINOMA, RENAL CELL). Common clinical signs include HYPERTENSION and neurological dysfunctions. $8 eng 450 $a Cerebelloretinal Angiomatosis, Familial $5 e $8 eng 450 $a Lindau Disease $5 e $8 eng 450 $a angiomatóza cerebeloretinálna familiárna $5 e $8 slo 450 $a Lindauova choroba $5 e $8 slo 450 $a Hippelova-Lindauova choroba $5 e $8 slo 450 $a Hippel-Lindauova choroba $5 e $8 slo 450 $a angiomatosis retinae $5 e $8 slo 450 $a angiomatosis retinocerebellosa $5 e $8 slo 450 $a von Hippelov-Lindauov syndróm $5 e $8 slo 450 $a VHL syndróm $5 e $8 slo 686 $a C10.562.925 686 $a C14.907.077.925 686 $a C16.131.077.245.750 686 $a C16.320.184.750 750 $a von Hippel-Lindau Disease $8 eng 801 -0
$a US $b DNLM $c 19990101 801 -2
$a SK $b BA006 $c 20010702 801 -2
$a SK $b BA006 $c 20080718 801 -2
$a SK $b BA006 $c 20211102 801 -2
$a SK $b BA006 $c 20221228 980 $x M
Počet záznamov: 1